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trial for assessing efficacy of treating anxiety in hypertensive patients.

Randomized Controlled Trial of Pharmacotherapy for Anxiety in Hypertensive Patients on Multiple Antihypertensive Drugs - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093930
Enrollment
105
Registered
2025-08-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I10- Essential (primary) hypertension

Interventions

Intervention1: pharmacotherapy: pharmacotherapy for anxiety ( Tab escitalopram ) + pharmacotherapy for hypertension for a total duration of 12 weeks Control Intervention1: pharmacotherapy: pharmacothe

Sponsors

All india institue of medical sciences, New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Hypertensive patients on at least 2 anti hypertensives. 2. Diagnosed with generalized anxiety disorder according to the DSM-5 criteria 3.Patient in the mild to moderate category of GAD (HAM A less than 25)

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. Patients with functional disability due ot anxiety. 2. Long QTc on Baseline ECG, or concomitant QTc prolonging drugs. 3. Patients with a primary psychiatric diagnosis other than anxiety disorder will be excluded, including patients with MDD (major depressive diorder), PTSD (post traumatic stress disorder), OCD (obsessive compulsive disorder), or any of the following DSM-5 diagnoses: 1) Dementia, delirium; 2) Schizophrenia, Schizoaffective, or other psychotic disorder; 3) Psychotic features including any delusions or hallucinations. 4. Patients with secondary causes of hypertension. 5. Current alcohol or other substance abuse disorder. 6. Patient taking herbal supplements. 7. Pregnant and lactating females will be excluded.

Design outcomes

Primary

MeasureTime frame
Change in anxiety symptoms as assessed by Hamilton Anxiety Rating scale (HAM-A).Timepoint: 4 weeks, 12 weeks

Secondary

MeasureTime frame
Change in blood pressure controlTimepoint: 4 weeks, 12 weeks;adverse eventsTimepoint: 4 weeks, 12 weeks;change in quality of life assessed by WHOQOL-BREF questionnaireTimepoint: 4 weeks, 12 weeks

Countries

India

Contacts

Public ContactDaksh Bansal

AIIMS New Delhi

rakeshyadav123@yahoo.com9868026888

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026